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作 者:Jayant I.Gowda Sharanappa T.Nandibewoor
机构地区:[1]P.G.Department of Studies in Chemistry,Karnatak University,Dharwad 580003,Indi
出 处:《Asian Journal of Pharmaceutical Sciences》2014年第1期42-49,共8页亚洲药物制剂科学(英文)
基 金:One of the author(J.I.Gowda)thanks UGC,New Delhi,for the award of Research Fellowship in Science for Meritorious Stu-dents(RFSMS).
摘 要:The electrochemical behavior of paclitaxel drug was studied at a glassy carbon electrode in phosphate buffer solutions using cyclic and differential-pulse voltammetric techniques.The oxidation process was shown to be irreversible over the pH range(3.0e10.4)and was diffusion controlled.Effects of anodic peak potential(E_(p)),anodic peak current(Ipa),scan rate,pH,heterogeneous rate constant(k^(0)),etc have been discussed.A possible electrooxidation mechanism was proposed.An analytical method was developed for the determination of paclitaxel in phosphate buffer solution at pH¼7.0 as a supporting electrolyte.The anodic peak current varied linearly with paclitaxel concentration in the range 1.0×10^-(6)M to 1.0×10^-(5)M with a limit of detection(LOD)of 1.23×10^(-8)M and limit of quantification(LOQ)of 4.10×10^(-8)M.The proposed method was successfully applied to the determination of paclitaxel in pure and real samples.
关 键 词:PACLITAXEL Glassy carbon electrode VOLTAMMETRY Injection analysis URINE
分 类 号:TG1[金属学及工艺—金属学]
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